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V C Sheffield

Showing results (21-30 of 153) with videos related to

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Progress in Clinical and Biological Research|January 1, 1982
Gene expression during chick limb cartilage differentiationW B Upholt, D Kravis, L Sandell, et al.
American Journal of Human Genetics|February 1, 1997
Improved set of short-tandem-repeat polymorphisms for screening the human genomeB Yuan, D Vaske, J L Weber, et al.
The Journal of Clinical Investigation|November 1, 1992
Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patientsE Freneaux, V C Sheffield, L Molin, et al.
Human Molecular Genetics|September 1, 1996
Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D)V Ionasescu, C Searby, V C Sheffield, et al.
Human Molecular Genetics|April 1, 1996
A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman IslandsA Nystuen, P J Benke, J Merren, et al.
Nature Genetics|April 7, 1999
The Pendred syndrome gene encodes a chloride-iodide transport proteinD A Scott, R Wang, T M Kreman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1991
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
Nature Genetics|July 1, 1992
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13E M Stone, B E Nichols, L M Streb, et al.
American Journal of Human Genetics|August 1, 1996
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindredsD A Scott, R Carmi, K Elbedour, et al.
American Journal of Human Genetics|August 27, 1998
Comprehensive human genetic maps: individual and sex-specific variation in recombinationK W Broman, J C Murray, V C Sheffield, et al.
Pageof 16

Showing results (21-30 of 153) with videos related to

Sort By:
Pageof 16
Progress in Clinical and Biological Research|January 1, 1982
Gene expression during chick limb cartilage differentiationW B Upholt, D Kravis, L Sandell, et al.
American Journal of Human Genetics|February 1, 1997
Improved set of short-tandem-repeat polymorphisms for screening the human genomeB Yuan, D Vaske, J L Weber, et al.
The Journal of Clinical Investigation|November 1, 1992
Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patientsE Freneaux, V C Sheffield, L Molin, et al.
Human Molecular Genetics|September 1, 1996
Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D)V Ionasescu, C Searby, V C Sheffield, et al.
Human Molecular Genetics|April 1, 1996
A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman IslandsA Nystuen, P J Benke, J Merren, et al.
Nature Genetics|April 7, 1999
The Pendred syndrome gene encodes a chloride-iodide transport proteinD A Scott, R Wang, T M Kreman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1991
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
Nature Genetics|July 1, 1992
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13E M Stone, B E Nichols, L M Streb, et al.
American Journal of Human Genetics|August 1, 1996
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindredsD A Scott, R Carmi, K Elbedour, et al.
American Journal of Human Genetics|August 27, 1998
Comprehensive human genetic maps: individual and sex-specific variation in recombinationK W Broman, J C Murray, V C Sheffield, et al.
Pageof 16